FdaApplication
ANDA 211242
Identifiers
- fda_app_no: ANDA211242
Properties
| Property | Value |
|---|---|
| applicant_name | MYLAN LABORATORIES LTD |
| application_type | ANDA |
| approval_date | 2018-10-04 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NOREPINEPHRINE BITARTRATE | NOREPINEPHRINE BITARTRATE | EQ 1MG BASE/ML | INJECTABLE;INJECTION |
1 product